Canonical Allele Identifier: CA2669052806
Gene: CLDN1 HGNC NCBI
CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190310258A>G , CM000665.2:g.190310258A>G GRCh38
NC_000003.11:g.190028047A>G , CM000665.1:g.190028047A>G GRCh37
NC_000003.10:g.191510741A>G NCBI36
NG_021418.1:g.17189T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295522.4:c.389-5T>C (CLDN1) MANE Select ENSP00000295522.3:n.389-5T>C
ENST00000295522.3:c.389-5T>C (CLDN1) ENSP00000295522.3:n.389-5T>C
ENST00000490800.1:n.348-5T>C (CLDN1)
NM_021101.4:c.389-5T>C (CLDN1) NP_066924.1:n.389-5T>C
XR_001741069.1:n.203-4635A>G
NM_021101.5:c.389-5T>C (CLDN1) MANE Select NP_066924.1:n.389-5T>C
NM_001378492.1:c.-445-4635A>G (CLDN16) NP_001365421.1:n.-445-4635A>G
NM_001378493.1:c.-279+19667A>G (CLDN16) NP_001365422.1:n.-279+19667A>G